Publications associated with Biological Physics


A pharmacological master key mechanism that unlocks the selectivity filter gate in K+ channels

Science American Association for the Advancement of Science 363 (2019) 875-880

ACW Pike, C Constantin, F Schulz, KS Vowinkel, LJ Conrad, W Gonzalez, AK Kiper, M Musinszki, M Tegtmeier, DC Pryde, H Belabed, M Nazare, BL De Groot, N Decher, B Fakler, EP Carpenter, S Tucker, T Baukrowitz, M Schewe, H Sun, Ü Mert, A Mackenzie

<jats:p>Potassium (K<jats:sup>+</jats:sup>) channels have been evolutionarily tuned for activation by diverse biological stimuli, and pharmacological activation is thought to target these specific gating mechanisms. Here we report a class of negatively charged activators (NCAs) that bypass the specific mechanisms but act as master keys to open K<jats:sup>+</jats:sup> channels gated at their selectivity filter (SF), including many two-pore domain K<jats:sup>+</jats:sup> (K<jats:sub>2P</jats:sub>) channels, voltage-gated hERG (human ether-à-go-go–related gene) channels and calcium (Ca<jats:sup>2+</jats:sup>)–activated big-conductance potassium (BK)–type channels. Functional analysis, x-ray crystallography, and molecular dynamics simulations revealed that the NCAs bind to similar sites below the SF, increase pore and SF K<jats:sup>+</jats:sup> occupancy, and open the filter gate. These results uncover an unrecognized polypharmacology among K<jats:sup>+</jats:sup> channel activators and highlight a filter gating machinery that is conserved across different families of K<jats:sup>+</jats:sup> channels with implications for rational drug design.</jats:p>


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